{
    "disease_id": "DOID:0060469", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "MDLS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "monosomy 17p13.3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "Miller-Dieker syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "telomeric deletion 17p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "Miller-Dieker syndrome chromosome region"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "lissencephaly due to 17p13.3 deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "MDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "chromosome 17P13.3 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009532", 
            "name": "MILLER-Dieker lissencephaly syndrome; MDLS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060469", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060469", 
            "name": "MDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060469", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060469", 
            "name": "Miller-Dieker syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060469", 
        "description": "A syndrome characterized by classical lissencephaly and distinct facial features and has_material_basis_in submicroscopic deletions of 17p13.3, including the LIS1 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060469", 
        "name": "Miller-Dieker lissencephaly syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/247200", 
            "id": "247200", 
            "database": "MIM"
        }
    ]
}